rs63750604

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;G)	6	Lynch syndrome, pathogenic mutation
(G;G)	0	common in clinvar

Make rs63750604(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37047577

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750604
dbSNP (classic)	rs63750604
ClinGen	rs63750604
ebi	rs63750604
HLI	rs63750604
Exac	rs63750604
Gnomad	rs63750604
Varsome	rs63750604
LitVar	rs63750604
Map	rs63750604
PheGenI	rs63750604
Biobank	rs63750604
1000 genomes	rs63750604
hgdp	rs63750604
ensembl	rs63750604
geneview	rs63750604
scholar	rs63750604
google	rs63750604
pharmgkb	rs63750604
gwascentral	rs63750604
openSNP	rs63750604
23andMe	rs63750604
SNPshot	rs63750604
SNPdbe	rs63750604
MSV3d	rs63750604
GWAS Ctlg	rs63750604

Max Magnitude

6

ClinVar
Risk	rs63750604(A;A)
Alt	rs63750604(A;A)
Reference	Rs63750604(G;G)
Significance	Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000003.11:g.37089068G>A
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075365.2, RCV000479277.1,